Poland· PL-100412886
Soledum forte
A cineole product containing cineolum, registered in Poland by M.C.M. Klosterfrau Healthcare Sp. z o.o.. The same ATC class is registered in 4 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Cineole is registered in 4 of 19 countries.
Countries holding a registration under ATC R05CA13 (cineole), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 3 of them publish a price we can compare per daily dose
Cineole · ATC R05CA13
4 / 19 countries
- Czechiaprice
- Germany
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Cineolum
- Manufacturer
- M.C.M. Klosterfrau Healthcare Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- R05CA13
- ATC class
- Cineole
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 3
- gtin05909991409807
- gtin05909991409814
- gtin05909991409821
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Cineole in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandPulmex SinuBronch 200 mg, magensaftresistente WeichkapselnSpirig HealthCare AG
- GermanyCineolG. Pohl-Boskamp Gmbh Co. Kg
- CzechiaSOLEDUMCassella-med GmbH & Co. KG, Kolín nad Rýnem
- BelgiumEucalyptine Lebrun Kinderen 5 mg - 80 mgMedgenix Benelux
Authorised across Europe · EMA
The same active substance is authorised in 7 EEA countries. Names it is sold under:
- Austria · Cinolpro, Cinolpro Forte
- Czechia · Soledum
- Germany · Cineol, Cinolpro
- Hungary · Soledum
- Romania · Soledum
- Slovenia · Soledum
- Slovakia · Soledum
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of URPL (Poland). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/c8b18ce3-bdd7-4c5f-9e64-45e96b385b7d GET /v1/drugs/c8b18ce3-bdd7-4c5f-9e64-45e96b385b7d?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"form": "Kapsułki dojelitowe miękkie",
"source": "urpl",
"strength": "200 mg",
"packaging": "05909991409807 ¦ OTC ¦ 133439\n20 kaps.\n05909991409814 ¦ OTC ¦ 133440\n50 kaps.\n05909991409821 ¦ OTC ¦ 133441\n100 kaps.",
"substance": "Cineolum 200 mg",
"common_name": "Cineolum",
"pl_product_id": "100412886",
"pozwolenie_nr": "25445",
"auth_procedure": "NAR",
"authorisation_validity": "Bezterminowe"
}See everything about cineole.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.